| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:186376014-186376132 | Common:1; Rare:27 | ||||
| chr1:186680121-186680844 | Common:4; Rare:176 | ||||
| chr1:186680891-186680952 | Common:1; Rare:14 | ||||
| chr1:192808588-192809111 | Common:5; Rare:182 | ||||
| chr1:192809397-192809486 | Rare:19 | ||||
| chr1:193058781-193058930 | Common:1; Rare:22 | ||||
| chr1:193059244-193059671 | Rare:199 | ||||
| chr1:193059988-193060209 | Rare:70 | ||||
| chr1:193105052-193105185 | Rare:24 | ||||
| chr1:193105269-193105725 | Common:4; Rare:185 | ||||
| chr1:193121639-193121815 | Common:2; Rare:68 | ||||
| chr1:193121845-193122218 | Common:1; Rare:118; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr1:193122292-193122487 | Rare:69; Clinvar:1 | ||||
| chr1:197146202-197146278 | Common:1; Rare:23; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:197146387-197146484 | Rare:39; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 |